Active Ingredient
Active ingredients: Alcohol 70.0%
Diiz Hand Sanitizer
FDA Label NDC 74923-080
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Sun Co.ltd for the product Diiz Hand Sanitizer (NDC 74923-080). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, inactive ingredient, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredients:
Aloe Barbadensis Leaf Extract, Citrus Paradisi (Grapefruit) Seed Extract, Disodium EDTA, Glycerin, Propylene Glycol, Carbomer, 1,2-Hexandiol, Water, Triethanolamine
Purpose
PURPOSE: Antimicrobial
Warnings
Warnings:
For external use only
Flammable. Keep away from heat and flame.
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if skin irritation or rash develops.
Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Uses
Uses
■ Hand sanitizer to reduce bacteria on the skin.
Directions
Directions
■ Put enough product in your palm to cover hands and rub hands together briskly until dry.
■ Children under 6 years of age should be supervised when using product.
Other Information
Other Information
■ Store below 43°C (110°F)
■ May discolor certain fabrics or surfaces
Questions
Questions
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